USH2A c.7783G>A ;(p.A2595T)

Variant ID: 1-216062208-C-T

NM_206933.2(USH2A):c.7783G>A;(p.A2595T)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Dependable and Efficient Clinical Molecular Diagnosis of Chinese RP Patient with Targeted Exon Sequencing.

Plos One
Yang, Liping L; Cui, Hui H; Yin, Xiaobei X; Dou, Hongliang H; Zhao, Lin L; Chen, Ningning N; Zhang, Jinlu J; Zhang, Huirong H; Li, Genlin G; Ma, Zhizhong Z
Publication Date: 2015

Variant appearance in text: USH2A: 7783G>A; A2595T
PubMed Link: 26496393
Variant Present in the following documents:
  • Main text
  • pone.0140684.s004.xlsx, sheet 3
  • pone.0140684.pdf
View BVdb publication page